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Underwater Field Guide to Ross Island & McMurdo 
Sound, Antarctica, Volume 4: Echinodermata 
seastars, urchins, brittle stars, sea cucumbers, crinoids 


Peter Brueggeman 


Photographs: Isidro Bosch, Peter Brueggeman, Rod Budd/Antarctica New 
Zealand, Kathleen Conlan/Canadian Museum of Nature, Paul Cziko, Paul 
Dayton, Shawn Harper, Henry Kaiser/NSF, Adam G Marsh, Jim Mastro, 

Bruce A Miller, Rob Robbins, Steve Rupp/NSF, M Dale Stokes, & Norbert 


N 
Ross Island & McMurdo Sound 


The National Science Foundation's Office of Polar Programs sponsored Norbert Wu on an Artist's 
and Writer's Grant project, in which Peter Brueggeman participated. One outcome from Wu's 
endeavor is this Field Guide, which builds upon principal photography by Norbert Wu, with photos 
from other photographers, who are credited on their photographs and above. This Field Guide aims 
to facilitate underwater/topside field identification from visual characters. Most organisms were 
identified from photographs with no specimen collection, so there can be uncertainty with these 
identifications. 


Seastar ID advisors included John H. Dearborn 
Taxonomic names checked in Zoological Record and World Register of Marine Species: October 2024 


Keywords; Antarctic, Antarctica, field guide, marine, Ross Island, McMurdo Sound, echinodermata, echinoderm, seastar, starfish, sea urchin, brittle star, sea cucumber, 
crinoid 


© 2024, first edition published in 1998. Text © Peter Brueggeman. Photographs © Isidro Bosch, Peter Brueggeman, Rod Budd/Antarctica New Zealand Pictorial Collection 
159679 2001-2002, Kathleen Conlan/Canadian Museum of Nature, Paul Cziko, Paul Dayton, Shawn Harper, Henry Kaiser/NSF, Adam G Marsh, Jim Mastro, Bruce A 
Miller, Rob Robbins, Steve Rupp/NSF, M Dale Stokes, & Norbert Wu. Photographs may not be used in any form without the express written permission of the 
photographers. Norbert Wu does not grant permission for uncompensated use of his photos; see www.norbertwu.com 


seastar Acodontaster conspicuus 


seastar Acodontaster hodgsoni 


seastar Cuenotaster involutus 


seastar Diplasterias brucei 


seastar Lophaster gaini 


seastar Macroptychaster accrescens 


astropectinid sea star, probably Macroptychaster accrescens or 
Leptychaster sp. 


seastar Notasterias armata 


seastar Odontaster spp. 


seastar Odontaster validus 


seastar Perknaster aurorae 


seastar Perknaster fuscus 


seastar Glabraster antarctica 


seastar Psilaster charcoti 


possibly the seastar Preraster affinis 


heart urchin Abatus sp. 


@ M Dale stokes 


pencil urchin Ctenocidaris perrieri 


sea urchin Sterechinus neumayeri 


brittle star Astrotoma agassizii 


brittle star Ophiacantha antarctica 


brittle star Ophionotus victoriae 


brittle star Ophioplinthus sp., probably Ophioplinthus gelida 


brittle star Ophiosparte gigas 


sea cucumber Staurocucumis liouvillei 


sea cucumber Staurocucumis turqueti 


sea cucumber Bathyplotes bongraini 


sea cucumber Cucumaria spp. 


sea cucumber Echinopsolus acanthocola 


sea cucumber Heterocucumis steineni 


@® Peter Urueqgeman 


sea cucumber, group Aspidochirotida 


crinoid Promachocrinus kerguelensis 


seastar Acodontaster conspicuus 


A. conspicuus 


Acodontaster conspicuus is 
found throughout Antarctica 
and the Antarctic Peninsula, 
South Shetland Islands, South 
Orkney Islands, South 
Sandwich Islands, South 
Georgia Island, Bouvet Island, 
and Falkland Islands between 0 
and 761+ meters depth 3,5 ,6,7,3}. 


Acodontaster conspicuus has 
been collected at sizes up to 
fourteen centimeters in radius 
from its center to the tip of an 
arm [4,6]. 


; The color of Acodontaster 


conspicuus (shown on the 
right compared to A. hodgsoni 


| on the left) has been recorded 
__ as pink, orange, pale orange, 
) brown, and brownish yellow 


and it may be yellowish 
towards the edges {4,6}. 


Acodontaster conspicuus has a 
flattened disc with arms wide 
at their base and narrowing 
quickly with a thin edge {«). 


10 


One way to distinguish Acodontaster conspicuus from 
the other Ross Sea Acodontaster species is by the 
presence of pincer-like pedicellariae on the underside 
of Acodontaster conspicuus {4}. 


; fe A preserved specimen of Acodontaster conspicuus shows 
the pincer-like pedicellariae with greater clarity (4). 


Pedicellaria keep the seastar's body surface clear of 


encrusting organisms by pinching or cutting their settling 
larvae. 


11 


©Norbert Wu 


Showing an Acodontaster sp. here, Acodontaster conspicuus is a predator of rossellid sponges and the sponges 
Homaxinella balfourensis, Anoxycalyx (Scolymastra) joubini (shown here), Antarctotetilla leptoderma, Haliclona 
scotti, Mycale (Oxymycale) acerata, and Kirkpatrickia variolosa {1,2}. Observations suggest that a single A. 
conspicuus does not stay long on the sponge Anoxycalyx (Scolymastra) joubini but several accumulate, do not 
leave, and consume enough of the sponge to kill it (2). 


12 


©Norbert Wu 


Here’s a gang attack on an Acodontaster sp. by the predatory seastar Odontaster validus. Predators of Acodontaster 
conspicuus include the seastar Odontaster validus (shown here), the nemertean proboscis worm Parborlasia 
corrugatus (in foreground), and the anemone Urticinopsis antarcticus {2,31}. Acodontaster conspicuus would reach 
population densities destroying the sponge community if not kept in check by Odontaster validus which preys upon 
the larvae, young and adult A. conspicuus {2}. A single Odontaster validus climbs up onto an Acodontaster 
conspicuus armray, everts its stomach, and digests a hole into it. An attack by a single Odontaster validus isn't fatal 
but nearby O. validus probably respond to the release of Acodontaster conspicuus coelomic fluid and join the attack 
[2]: 


13 


QNorbert 


Showing an Acodontaster sp. here, a gang attack eventually slows the larger Acodontaster conspicuus seastar's 
movement, more Odontaster validus join the attack, and the large nemertean proboscis worm Parborlasia 
corrugatus joins in as well. A. conspicuus seastars can become completely buried under high piles of attacking 
Odontaster validus seastars and Parborlasia corrugatus worms 2}. 


References: 1: Science 245:1484-1486, 1989; 2: Ecological Monographs 44(1):105-128, 1974 (P. Dayton, personal communication, 2015: Haliclona dancoi observations are 
corrected to H. scotti; Rossella racovitzae observations are corrected to R. podagrosa); 3: Adaptations within Antarctic Ecosystems: Proceedings of the Third SCAR 
Symposium on Antarctic Biology. George A. Llano, ed. Washington: Smithsonian Institution; Houston, Tex.: distributed by Gulf Pub. Co., 1977. pp.293-326; 4: The Fauna 
of the Ross Sea, Part 3, Asteroidea. HES Clark. New Zealand Department of Scientific and Industrial Research Bulletin 151, New Zealand Oceanographic Institute Memoir 
21, 1963; 5: Polar Biology 20(4):229-247, 1998; 6: Equinodermos Antarticos. II. Asteroideos. 5. Asteroideos de la Extremidad Norte de la Peninsula Antartica. I Bernasconi. 
Revista del Museo Argentino de Ciencias Naturales "Bernardino Rivadavia" e Instituto Nacional de Investigacion de las Ciencias Naturales. Zoologia (aka Ciencias 
Zoologicas) 9(10):211-281 and plates, 1970; 7: U.S. National Museum of Natural History, Dept of Zoology, Invertebrate Zoology, Invertebrate Zoology Collections 
database; 8: Amazing Antarctic asteroids: a guide to the starfish of the Ross Sea. Kate Neill et al. NIWA, New Zealand, Version 1, 2016 www.niwa.co.nz/coasts-and- 
oceans/marine-identification-guides-and-fact-sheets/amazing-antarctic-asteroids 


14 


seastar Acodontaster hodgsoni 


Acodontaster hodgsoni is found throughout 
Antarctica, the Antarctic Peninsula, South 
Shetland Islands, South Orkney Islands, South 
Sandwich Islands, South Georgia Island, 
Bouvet Island, Crozet Islands, Heard Island, 
Kerguelen Islands, Prince Edward Islands, 


9 9'F Vy 


Acodontaster hodgsoni has been collected 
at sizes up to twenty centimeters in radius 
from its center to the tip of an arm /2}. 


15 


A. conspicuus 


Acodontaster hodgsoni is shown on 
the left compared to Acodontaster 
conspicuus on the right. 


Acodontaster hodgsoni is a predator 
of the sponges Haliclona scotti, 
Calyx shackletoni, rossellid 
sponges, and Hemigellius fimbriatus 


[1]. 


As shown here, Acodontaster 
hodgsoni lacks the pincer-like 
pedicellariae alongside its 
underside spines, which are present 
on Acodontaster conspicuus {2}. 


Predators of Acodontaster hodgsoni include the seastar Odontaster validus, the nemertean worm Parborlasia 


corrugatus, and the anemone Urticinopsis antarcticus {1}. 


References: 1: Ecological Monographs 44(1):105-128, 1974 (P. Dayton, personal communication, 2015: Haliclona dancoi observations are corrected to H. scotti; Gellius 
tenella corrected to Hemigellius fimbriatus; Rossella racovitzae observations are corrected to R. podagrosa); 2: The Fauna of the Ross Sea, Part 3, Asteroidea. HES Clark. 
New Zealand Department of Scientific and Industrial Research Bulletin 151, New Zealand Oceanographic Institute Memoir 21, 1963; 3: Bulletin de l'Institut Royal des 
Sciences Naturelles de Belgique. Biologie 63:175-184, 1993; 4: Discovery Reports 20:115, 1941; 5: U.S. National Museum of Natural History, Dept of Zoology, Invertebrate 
Zoology, Invertebrate Zoology Collections database; 6: Polar Biology 38:799-813, 2015; 7: Amazing Antarctic asteroids: a guide to the starfish of the Ross Sea. Kate Neill et 
al. NIWA, New Zealand, Version 1, 2016 www.niwa.co.nz/coasts-and-oceans/marine-identification-guides-and-fact-sheets/amazing-antarctic-asteroids 


16 


seastar Cuenotaster involutus 


@Canadian Museuii"ot) Ale oa 


Cuenotaster involutus is found throughout Antarctica and the Antarctic Peninsula, South Shetland Islands, South 
Orkney Islands, South Georgia Island, Shag Rocks, and Bouvet Island from 0 to 794 meters depth [1,2,4,5,6,7]. 


The disc of C. involutus may be flat or slightly convex and is depressed between arms [3]. The arms of Cuenotaster 
involutus are long, slender, flexible, convex-surfaced, and blunt-tipped and may sometimes be coiled ventrally [3,4). 


Cuenotaster involutus has been collected at sizes up eleven centimeters in radius from its center to the tip of an arm 
[23,5] 


17 


aNorbett 


The color of Cuenotaster involutus includes pink-brick, grey-brown, yellowish brown, white, greenish gray, and 
gray white [2,3,4,5). 


Cuenotaster involutus has distinctive and unmistakeable bristling, and well-spaced rosette-like paxillae along the 
disc and arms of Cuenotaster involutus (3,4,5}. 


Cuenotaster involutus may be both an active predator and a scavenger [1). 


References: 1: Adaptations within Antarctic Ecosystems: Proceedings of the Third SCAR Symposium on Antarctic Biology. George A. Llano, ed. Washington: Smithsonian 
Institution; Houston, Tex.: distributed by Gulf Pub. Co., 1977. pp.293-326; 2: Fauna der Antarktis. J Sieg & JW Wagele, eds. Berlin: P. Parey, 1990; 3: The Fauna of the 
Ross Sea, Part 3, Asteroidea. HES Clark. New Zealand Department of Scientific and Industrial Research Bulletin 151, New Zealand Oceanographic Institute Memoir 21, 
1963; 4: Discovery Reports 20:69-306 and plates, 1940; 5: Equinodermos Antarticos. II. Asteroideos. 5. Asteroideos de la Extremidad Norte de la Peninsula Antartica. I 
Bernasconi. Revista del Museo Argentino de Ciencias Naturales "Bernardino Rivadavia" e Instituto Nacional de Investigacion de las Ciencias Naturales. Zoologia (aka 
Ciencias Zoologicas) 9(10):211-281 and plates, 1970; 6: Polar Biology 38:799-813, 2015; 7: Amazing Antarctic asteroids: a guide to the starfish of the Ross Sea. Kate Neill 
et al. NIWA, New Zealand, Version 1, 2016 www.niwa.co.nz/coasts-and-oceans/marine-identification-guides-and-fact-sheets/amazing-antarctic-asteroids 


18 


seastar Diplasterias brucei 


Diplasterias brucei is found throughout Antarctica and the Antarctic Peninsula, South Shetland Islands, South 
Orkney Islands, South Sandwich Islands, South Georgia Island (six-rayed forma), Tierra del Fuego, Crozet Islands, 
Heard Island, Marion and Prince Edward Islands, from 0 to 752 meters depth [3,6,7,8,9,10,11,12}- 


19 


Diplasterias brucei color can be light blue-green on top with white spines and a whitish border to the disc and arms 
with the arm tips blood-red; other recorded colors are pale grey to blue-grey, pale orange or pale blue-grey with a 
red eye spot at each arm tip, light brown, creamy white with red blotches ,7,10}. 


©Norbert Wu 


The disc of Diplasterias brucei is small and convex; its arms taper gradually to blunt tips (7). Diplasterias brucei has 
been collected at sizes up to 23.7 centimeters in radius from its center to the tip of an arm [6,7,10}. 


21 


These are juvenile 
Diplasterias brucei. 


22 


@Norbert. Wu 


As shown here, Diplasterias brucei specializes on molluscan prey; it is a significant predator of the bivalve mollusc 
Limatula hodgsoni which can comprise almost all of its diet (2,3). Diplasterias brucei also eats the muricid gastropod 
Trophonella longstaffi, and is a scavenger on dead material (2,3). 


Diplasterias brucei is a prey item for the anemone Urticinopsis antarctica (2). 


23 


Here is Diplasterias brucei on anchor ice. 


24 


Here Diplasterias brucei is humped up and brooding its young in a pocket formed by the underside of its body [1). 
Ripe females have been observed year-round |5}. 


25 


Closer view of the eggs being brooded by Diplasterias brucei, as seen from its underside, the ventral side of the 
seastar. 


Brood protection occurs quite commonly among Antarctic marine invertebrates (4). 


©Bruce A Miller 


This Diplasterias brucei is humped up and brooding its young. 


21 


Yolky eggs of Diplasterias brucei. 


Brood protection helps larvae avoid the stresses of the environment and predation {4}. Brooding helps larvae avoid 
the dangers of being eaten if the larvae were planktonic in a strong seasonal planktonic cycle as seen in Antarctic 
waters [4). 


References: 1: Ecological Monographs 44(1):105-128, 1974; 2: Antarctic Ecology, Volume 1. MW Holdgate, ed. NY: Academic Press, 1970. pp.244-258; 3: Adaptations 
within Antarctic Ecosystems: Proceedings of the Third SCAR Symposium on Antarctic Biology. George A. Llano, ed. Washington: Smithsonian Institution; Houston, Tex.: 
distributed by Gulf Pub. Co., 1977. pp.293-326; 4: Adaptations within Antarctic Ecosystems: Proceedings of the Third SCAR Symposium on Antarctic Biology. George A. 
Llano, ed. Washington: Smithsonian Institution; Houston, Tex.: distributed by Gulf Pub. Co., 1977. pp.135-157; 5: Marine Biology 104: 41-46, 1990; 6: Fauna der Antarktis. 
J Sieg & JW Wagele, eds. Berlin: P. Parey, 1990; 7: The Fauna of the Ross Sea, Part 3, Asteroidea. HES Clark. New Zealand Department of Scientific and Industrial 
Research Bulletin 151, New Zealand Oceanographic Institute Memoir 21, 1963; 8: AM Clark. B.A.N.Z. Antarctic Research Expedition 1929-1931. Reports, Series B 
(Zoology and Botany) Volume 9, Asteroidea. Adelaide: BANZAR Expedition Committee, 1962; 9: Discovery Reports 20:69-306 and plates, 1940; 10: Equinodermos 
Antarticos. II. Asteroideos. 5. Asteroideos de la Extremidad Norte de la Peninsula Antartica. I Bernasconi. Revista del Museo Argentino de Ciencias Naturales "Bernardino 
Rivadavia" e Instituto Nacional de Investigacion de las Ciencias Naturales. Zoologia (aka Ciencias Zoologicas) 9(10):211-281 and plates, 1970; 11: Polar Biology 41:2423- 
2433, 2018; 12: Amazing Antarctic asteroids: a guide to the starfish of the Ross Sea. Kate Neill et al. NIWA, New Zealand, Version 1, 2016 www.niwa.co.nz/coasts-and- 
oceans/marine-identification-guides-and-fact-sheets/amazing-antarctic-asteroids 


28 


seastar Lophaster gaini 


Lophaster gaini is found throughout Antarctica and the Antarctic Peninsula, South Shetland Islands, and Adelaide 
Island, at depths from 23 to 578 meters 11,36). Lophaster gaini has been collected at sizes up to 17.5 centimeters in 
radius from its center to the tip of an arm 11). 


©Norbert Wu 


Lophaster gaini has a broad disc which is slightly concave in the center; its arms are broad at the base and taper 
evenly to blunt tips protected by small square plates [1}. 


30 


a1 


‘ae Rt. 
TARR 


ee 


One prey item of Lophaster gaini is the Antarctic scallop Adamussium colbecki {4}. 


References: 1: The Fauna of the Ross Sea, Part 3, Asteroidea. HES Clark. New Zealand Department of Scientific and Industrial Research Bulletin 151, New Zealand 
Oceanographic Institute Memoir 21, 1963; 2: Isidro Bosch, 1999, personal communication; 3: Jim Mastro, personal communication, 1999 (New Harbor, 23 meters); 4: 
Ecology of the Circumpolar Antarctic Scallop, Adamussium colbecki (Smith, 1902). Paul Arthur Berkman. Ph. D. Dissertation, University of Rhode Island, 1988; 5: 
Echinodermes (Asteries, Ophiures et Echinides). R Koehler. Deuxieme Expedition Antarctique Francaise (1908-1910) commandee par le Dr Jean Charcot. Sciences 
Naturelles. Documents Scientifiques. Paris: Masson et Cie, 1912; 6: Amazing Antarctic asteroids: a guide to the starfish of the Ross Sea. Kate Neill et al. NIWA, New 
Zealand, Version 1, 2016 www.niwa.co.nz/coasts-and-oceans/marine-identification-guides-and-fact-sheets/amazing-antarctic-asteroids 


seastar Macroptychaster accrescens 


Macroptychaster accrescens color has been recorded as orange with darker brown transverse bands across the arms 
and brown markings on the central disc ,1). 


33 


@Brtce A Miller 


Macroptychaster accrescens has been collected at sizes up to 26 centimeters in radius from its center to the tip of an 
arm [1]. 


Macroptychaster accrescens is uncommonly seen {4}. 


34 


Like other seastars in the Astropectinidae, Macroptychaster accrescens lacks sucking discs on its tube feet 
indicating a preference for soft or muddy environments 11}. 


@Bruce “A Miller 


Macroptychaster accrescens is a predator of the seastar Odontaster validus, the sea urchin Sterechinus neumayeri, 
gastropod molluscs, bivalves, and brittle stars (3,4). 


Females of Macroptychaster accrescens are presumed to spawn their eggs by broadcasting them into the water 
where they develop into non- feeding larvae [2). This pelagic (open ocean) non-feeding larval development is common 
among McMurdo Sound seastars |2). Their larvae develop on stored yolk (lecithotrophic) which is probably an 
adaptation to low food levels {2}. Seastars in temperate and tropical shallow waters typically have feeding larvae (2). 


36 


@Bruce ASMyliler 


References: 1: The Fauna of the Ross Sea, Part 3, Asteroidea. HES Clark. New Zealand Department of Scientific and Industrial Research Bulletin 151, New Zealand 
Oceanographic Institute Memoir 21, 1963; 2: Marine Biology 104:41-46, 1990; 3: Ecological Monographs 44(1):105-128, 1974; 4: Adaptations within Antarctic 
Ecosystems: Proceedings of the Third SCAR Symposium on Antarctic Biology. George A. Llano, ed. Washington: Smithsonian Institution; Houston, Tex.: distributed by 
Gulf Pub. Co., 1977. pp.293-326; 5: Equinodermos Antarticos. II. Asteroideos. 5. Asteroideos de la Extremidad Norte de la Peninsula Antartica. I Bernasconi. Revista del 
Museo Argentino de Ciencias Naturales "Bernardino Rivadavia" e Instituto Nacional de Investigacion de las Ciencias Naturales. Zoologia (aka Ciencias Zoologicas) 
9(10):211-281 and plates, 1970; 6: Amazing Antarctic asteroids: a guide to the starfish of the Ross Sea. Kate Neill et al. NIWA, New Zealand, Version 1, 2016 
www.niwa.co.nz/coasts-and-oceans/marine-identification-guides-and-fact-sheets/amazing-antarctic-asteroids; 7: Polish Polar Research 18(2):107-117, 1997 


37 


astropectinid sea star, probably Macroptychaster accrescens or Leptychaster sp. 


° 


@Norbert Wu 


These sea stars get very large and massive; this animal is probably a juvenile or young adult (1). Several characters 
place it in the Leptychaster - Leptoptychaster - Macroptychaster complex which isn't taxonomically well-defined; 
the species in these genera are fairly common on the Antarctic Shelf, but variable in their morphology {1}. 


References: 1: John H. Dearborn, personal communication, 1999 


38 


seastar Notasterias armata 


@Norbert Wu 


Notasterias armata is found throughout Antarctica and the Antarctic Peninsula, South Shetland Islands, Bouvet 
Island, and Kerguelen Islands, from 15 to 752 meters depth [1,2,7,3). 


39 


@Shawn Harper 


The color of Notasterias armata can be orange, creamy white, red, and mottled red with creamy areas (2,3). 
Notasterias armata has been collected at sizes up to thirteen centimeters in radius from its center to the tip of an 
arm 2,3]. The disc of Notasterias armata is small and its arms taper to blunt tips (2). 


40 


CON Fe bye FiaS ni 


The diet of Notasterias armata includes the Antarctic scallop Adamussium colbecki (shown here) as well as the 
bivalve Limatula hodgsoni {1,6}. 


Notasterias armata broods its young in a brooding posture with a strongly convex disc and supporting itself on 
bent arms [2]. Ripe females have been observed from August to February [5]. Brood protection occurs quite 
commonly among Antarctic marine invertebrates ,4}. Brood protection helps larvae avoid the stresses of the 
environment and predation {4}. Brooding helps larvae avoid the dangers of being eaten if the larvae were planktonic 
in a strong seasonal planktonic cycle as seen in Antarctic waters [4}. 


41 


References: 1: Adaptations within Antarctic Ecosystems: Proceedings of the Third SCAR Symposium on Antarctic Biology. George A. Llano, ed. Washington: Smithsonian 
Institution; Houston, Tex.: distributed by Gulf Pub. Co., 1977. pp.293-326; 2: The Fauna of the Ross Sea, Part 3, Asteroidea. HES Clark. New Zealand Department of 
Scientific and Industrial Research Bulletin 151, New Zealand Oceanographic Institute Memoir 21, 1963; 3: Fauna der Antarktis. J Sieg & JW Wagele, eds. Berlin: P. Parey, 
1990; 4: Adaptations within Antarctic Ecosystems: Proceedings of the Third SCAR Symposium on Antarctic Biology. George A. Llano, ed. Washington: Smithsonian 
Institution; Houston, Tex.: distributed by Gulf Pub. Co., 1977. pp.135-157; 5: Marine Biology 104: 41-46, 1990; 6: Ecology of the Circumpolar Antarctic Scallop, 
Adamussium colbecki (Smith, 1902). Paul Arthur Berkman. Ph. D. Dissertation, University of Rhode Island, 1988; 7: Mitteilungen aus dem Hamburgischen Zoologischen 
Museum und Institut 89:239- 259, 1992; 8: Amazing Antarctic asteroids: a guide to the starfish of the Ross Sea. Kate Neill et al. NIWA, New Zealand, Version 1, 2016 
www.niwa.co.nz/coasts-and-oceans/marine-identification-guides-and-fact-sheets/amazing-antarctic-asteroids 


42 


seastar Odontaster spp. 


@Peter Brueggeman 


In the Ross Sea, an Odontaster seastar with yellow coloration can be Odontaster roseus, O. pearsei, O. validus, or 
O. meridionalis [2,7,11,13,17,21]- 


Odontaster roseus can be yellow, rosy, drab red, or tan /13.17]. 
Odontaster pearsei can be yellow or orange to tan {13,17}. 


Odontaster validus varies widely in color and can be orange-yellow colored in addition to its characteristic dark 
pink/red color ,17;. Colors of O. validus include dark brown, purple, purple-red, orange, orange-yellow, red-orange, 
red, brick red, dark carmine, and pink [17,18,19,20}. 


Odontaster meridionalis color is variable and includes yellow-white, dirty yellow, orange yellow, bright orange, 
pale brown, and a grey center grading to white at arm tips [2,7). O. meridionalis is generally pale brown or yellowish 
white on the dorsal surface and lighter on the ventral surface {11}. 


43 


@Peter Brueggeman 


Odontaster roseus and Odontaster pearsei have been found in the Antarctic Peninsula and Terra Nova Bay [13.17}. 
A classification key for Odontaster species was published in 2010 {13}. Odontaster roseus, O. pearsei, and O. 
validus can be differentiated by the number of spines on abactinal plates and their length, and the marginal plates 
and spines, in addition to genetic sequences [17}. 


44 


Odontaster meridionalis is found throughout Antarctica and the Antarctic Peninsula, South Shetland Islands, South 
Sandwich Islands, South Georgia Island, Shag Rocks, Straits of Magellan, Tierra del Fuego, Bouvet Island, Marion 
and Prince Edward Islands, Kerguelen Islands, Crozet Islands, and Heard Island, from 0 to 647 meters depth 
[1,2,5,6,7,8,9,10,12,14,15,16]. Genetic study points to O. meridionalis in Kerguelen Islands and O. pencillatus in South 
America being a single species occurring in both regions (21). 


45 


Odontaster meridionalis has been collected at sizes up to nine centimeters in radius from its center to the tip of an 
arm [2]. O. meridionalis has a flattened disc with its arms narrowing down on the latter half of their length [g}. 


46 


@Norbert Wu 


Odontaster meridionalis is an important predator of the sponge Homaxinella balfourensis and also eats rossellid 
sponges and the sponges Haliclona scotti, Mycale (Oxymycale) acerata, Polymastia invaginata, Hemigellius 
fimbriatus, Isodictya setifera, and Pachychalina pedunculata {3,4. O. meridionalis is preyed upon by the anemone 
Urticinopsis antarcticus and the seastar Macroptychaster accrescens {5}. 


47 


” Photograph: Adam G. Marsh 
Af ZZ Copyright: 2007 


Female Odontaster meridionalis spawn their eggs by broadcasting them into the water where they develop into 
feeding larvae ,1). This differs from the more common tendency of McMurdo Sound seastars to have pelagic (open 
ocean) non-feeding larval development [1). 


48 


@Shawn Harper 


References: 1: Marine Biology 104:41-46, 1990; 2: The Fauna of the Ross Sea, Part 3, Asteroidea. HES Clark. New Zealand Department of Scientific and Industrial 
Research Bulletin 151, New Zealand Oceanographic Institute Memoir 21, 1963; 3: Science 245:1484-1486, 1989; 4: Ecological Monographs 44(1):105-128, 1974 (P. 
Dayton, personal communication, 2015: Haliclona dancoi observations are corrected to H. scotti; Gellius tenella corrected to Hemigellius fimbriatus; Rossella racovitzae 
observations are corrected to R. podagrosa); 5: Adaptations within Antarctic Ecosystems : Proceedings of the Third SCAR Symposium on Antarctic Biology. George A. 
Llano, ed. Washington: Smithsonian Institution; Houston, Tex. : distributed by Gulf Pub. Co., 1977. pp.293-326; 6: AM Clark. B.A.N.Z. Antarctic Research Expedition 
1929-1931. Reports, Series B (Zoology and Botany) Volume 9, Asteroidea. Adelaide: BANZAR Expedition Committee, 1962; 7: Discovery Reports 20:69-306 and plates, 
1940; 8: Equinodermos Antarticos. II. Asteroideos. 5. Asteroideos de la Extremidad Norte de la Peninsula Antartica. I Bernasconi. Revista del Museo Argentino de Ciencias 
Naturales "Bernardino Rivadavia" e Instituto Nacional de Investigacion de las Ciencias Naturales. Zoologia (aka Ciencias Zoologicas) 9(10):211-281 and plates, 1970; 9: 
South African Journal of Antarctic Research 23(1-2):37- 70, 1993; 10: Scientia Marina 63(Supplement 1):433-438, 1999; 11: John Dearborn, personal communication, 2001; 
12: Revista Ciencia y Tecnologia del Mar 29(1):91-102, 2006; 13: Integrative and Comparative Biology 50(6):981-992, 2010; 14: Polar Biology 38:799-813, 2015; 15: Polar 
Biology 41:2423-2433, 2018; 16: Amazing Antarctic asteroids: a guide to the starfish of the Ross Sea. Kate Neill et al. NIWA, New Zealand, Version 1, 2016 
www.niwa.co.nz/coasts-and-oceans/marine-identification-guides-and-fact-sheets/amazing-antarctic-asteroids 17: Diversity 14:457, 2022. doi.org/10.3390/d14060457; 18: 
The Fauna of the Ross Sea, Part 3, Asteroidea. HES Clark. New Zealand Department of Scientific and Industrial Research Bulletin 151, New Zealand Oceanographic 
Institute Memoir 21, 1963; 19: Discovery Reports 20:69-306 and plates, 1940; 20: Equinodermos Antarticos. II. Asteroideos. 5. Asteroideos de la Extremidad Norte de la 
Peninsula Antartica. I Bernasconi. Revista del Museo Argentino de Ciencias Naturales "Bernardino Rivadavia" e Instituto Nacional de Investigacion de las Ciencias 
Naturales. Zoologia (aka Ciencias Zoologicas) 9(10):211-281 and plates, 1970; 21: Diversity 15:1129, 2023. doi.org/10.3390/d15111129 


49 


seastar Odontaster validus 


4 > oy re . 1 IR 
UTA Bo” houa de> SS Ap boii * 


RIA wR SNA 


Zw, ipa be oa i OR HK Aa igo 
( Dene. aa Ain AATE™ y) 


Odontaster validus is found throughout Antarctica & the Antarctic Peninsula, South Shetland Islands, South 
ae Islands, South Sandwich Islands, South eee Island, Shag Rocks, Chile, Falkland Islands, Bouvet 


Reported distribution beyond Antarctica is not supported by mitochondrial DNA data, which shows Odontaster 
validus to be geographically isolated to Antarctic and subantarctic waters [21). 


@Shawn Harper 


. 


Odontaster validus has a broad disc and short arms tapering to blunt tips ,7}. O. validus varies in color including 
dark brown, purple, purple-red, orange, orange-yellow, red-orange, red, brick red, dark carmine, and pink; it may 
have light colored arm tips [7,11,14,22}. Odontaster validus is usually bright to dull red on the dorsal (abactinal) 
surface, and yellowish white to pale pink on the ventral (actinal) surface [16]. However O. validus can be orange- 
yellow colored on its dorsal surface in addition to its characteristic dark pink/red color, thus confounding visual 
identification by color for this species [22]. Odontaster validus, O. roseus, and O. pearsei can be differentiated by 
the number of spines on abactinal plates and their length, and the marginal plates and spines, in addition to genetic 
sequences |2). 


eH 


Odontaster validus has been collected at sizes up to seven centimeters in radius from center to arm tip 17,11). O. 
validus has a characteristic position with its arm tips slightly raised ,7}. 


52 


Here's a juvenile and adult of Odontaster validus. 


Size-frequency distribution of Odontaster validus can vary with location and is a reflection of the general level of 
productivity of a habitat: at McMurdo Station, their size and number decrease with depth; at Cape Evans, they are 
more numerous and generally smaller; and, at East Cape Armitage, they are less numerous and very small 13}. 


Odontaster validus is slow growing; well-fed individuals need about nine years to reach thirty grams wet weight 
which is near the mean size of shallow-water individuals at McMurdo Station [3]. Based on its growth rate, collected 
sizes, and knowledge from other seastars, O. validus may live beyond one hundred years of age, with very low 
turnover in a population 117). 


53 


CtNorbere’. Wu 


Here Odontaster validus is ganging up and eating the sea urchin Sterechinus neumayeri; little red amphipods are 
stealing food in the process. O. validus appears voracious, being very numerous in some areas and piled up in 
feeding groups; one study found that almost 50% of O. validus in the study area were engaged in feeding with their 
everted stomach 113}. 


Odontaster validus is omnivorous, capable of filter-feeding and eating a varied diet: detritus, small crustaceans 
including amphipods and the isopod Glyptonotus antarcticus, seastars, molluscs (scallop Adamussium colbecki, 
gastropods, bivalves Laternula elliptica and Limatula hodgsoni), hydroids (including Hydrodendron arboreum), bryozoans, sponges 
(rossellid sponges, Homaxinella balfourensis, Scolymastra joubini, Tetilla leptoderma), ostracods, sea urchin Sterechinus 
neumayeri, polychaete worms, carrion (including dead Weddell seals), feces (from Weddell seals), diatoms, and algae 
[5,8,9,13,15]. O. validus has been observed feeding on the detrital film on the surface of the sponge Cinachyra 
antarctica [13]. 


54 


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ao) 
uy 
iy) 
" 
0 
= 


56 


at 


Odontaster validus seastars piled up and feeding on Weddell seal feces under ice holes used by Weddell seals to 
enter and exit the water through the thick sea ice. 


58 


Odontaster validus is a prey item of the seastar Macroptychaster accrescens |;,and of the anemone Urticinopsis 
antarcticus {6}. 


Odontaster validus broadcast-spawns larvae which feed on bacteria and algae and have a low metabolic rate (which 
predicts long-term larval survival); larvae of a comparable temperate seastar eat only algae and have a higher 
metabolic rate /1,2}. 


39 


@Norbert Wu 


Here’s a gang attack on Acodontaster sp. seastar. A single Odontaster validus climbs up onto a ray of the seastar, 
everts its stomach, and digests a hole into it. An attack by a single O. validus isn't fatal but nearby O. validus 
probably respond to the release of coelomic fluid from the seastar and join the attack [5}. 


The seastars Odontaster validus and Acodontaster conspicuus are the two greatest predators on McMurdo sponges 
[5]: Odontaster validus is a foundation species in the McMurdo sponge-dominated benthic ecosystem and is the 
keystone to the interaction between the rossellid sponges and one of their primary predators, the large Antarctic 
seastar Acodontaster conspicuus {4}. A. conspicuus would reach population densities destroying the sponge 
community if not kept in check by O. validus which preys upon its larvae, young and adults [5}. 


60 


@QNorbert. Wu 


Showing an Acodontaster sp. seastar here, eventually the larger seastar's movement is slowed, and more Odontaster 
validus seastars attack. Seastars can become completely buried under high piles of attacking Odontaster validus 
seastars and Parborlasia corrugatus worms [5]. 


61 


rei 
al 
poe 
: 
= 
<4 
fie. 
“= 
Wi) 
od, 


Odontaster validus seastars attack an urchin. 


62 


@Adam:.:;Marsh 


Odontaster validus seastar eating a gorgonian. 


Odontaster validus is the most abundant seastar in the shallow shelf waters of Antarctica and is most abundant from 
15 to 200 meters {9}. 


TAXONOMIC NOTE: A classification key for Odontaster species was published in 2010 {13}. Three closely 
related species in Odontaster have been identified by molecular barcoding (O. validus, O. roseus, and O. pearsei), 
but morphological variation in a single population of Odontaster validus from one locality covers the whole range 
of that reported for O. roseus, and overlaps that of O. pearsei [18,1921]. Odontaster roseus, O. pearsei, and O. validus 
can be differentiated by the number of spines on abactinal plates and their length, and the marginal plates and 
spines, in addition to genetic sequences |23). 


63 


Photograph: Adam.G. Marsh 
Copyright: 2007 


References: 1: Antarctic Journal of the United States 26(5):170-172, 1991; 2: Antarctic Journal of the United States 26(5):163-165, 1991; 3: Marine Biology 99(2):235-246, 
1988; 4: Colloquium on Conservation Problems in Antarctica, Sept. 10-12, 1971, Blacksburg, VA, Proceedings. BC Parker, ed. Lawrence, Kansas, Allen Press, 1972. pp.81- 
96; 5: Ecological Monographs 44(1):105-128, 1974 (Paul Dayton, personal communication, 2015: Rossella racovitzae observations are corrected to R. podagrosa); 6: 
Antarctic Ecology, Volume 1. MW Holdgate, ed. NY: Academic Press, 1970. pp244- 258; 7: The Fauna of the Ross Sea, Part 3, Asteroidea. HES Clark. New Zealand 
Department of Scientific and Industrial Research Bulletin 151, New Zealand Oceanographic Institute Memoir 21, 1963; 8: Science 245:1484- 1486, 1989; 9: Adaptations 
within Antarctic Ecosystems: Proceedings of the Third SCAR Symposium on Antarctic Biology. GA Llano, ed. Washington: Smithsonian Institution; Houston, Tex.: 
distributed by Gulf Pub. Co., 1977. pp.293-326; 10: AM Clark. BANZ Antarctic Research Expedition 1929-1931. Reports, Series B (Zoology and Botany) Volume 9, 
Asteroidea. Adelaide: BANZAR Expedition Committee, 1962; 11: Discovery Reports 20:69-306 and plates, 1940; 12: South African Journal of Antarctic Research 23(1- 
2):37-70, 1993; 13: New Zealand Antarctic Record 9(2):34-52, 1989; 14: Equinodermos Antarticos. II. Asteroideos. 5. Asteroideos de la Extremidad Norte de la Peninsula 
Antartica. I Bernasconi. Revista del Museo Argentino de Ciencias Naturales "Bernardino Rivadavia" e Instituto Nacional de Investigacion de las Ciencias Naturales. 
Zoologia (aka Ciencias Zoologicas) 9(10):211-281 and plates, 1970; 15: Antarctic Science 12(1):64-68, 2000; 16: John Dearborn, personal communication, 2001; 17: 
Australian Natural History 16(7):234-238, 1969; 18: Integrative and Comparative Biology 50(6):981-992, 2010; 19: Polar Biology 41:2159-2165, 2018; 20: Amazing 
Antarctic asteroids: a guide to the starfish of the Ross Sea. Kate Neill et al. NIWA, New Zealand, Version 1, 2016 www.niwa.co.nz/coasts-and-oceans/marine-identification- 
guides-and-fact-sheets/amazing-antarctic-asteroids; 21: Polar Biology 34(4):575—586, 2011; 22: Diversity 14:457, 2022. doi.org/10.3390/d14060457 


64 


seastar Perknaster aurorae 


Perknaster aurorae is found in the Antarctic 
Peninsula, South Shetland Islands, South 
Sandwich Islands, South Georgia Island, and 
Shag Rocks, and probably throughout 
Antarctica, from 18 to 310 meters depth 11,4,5). 
P. aurorae has a large convex disc and long 
arms that are wide at the base [1). P. aurorae 
has been collected at sizes up to fourteen 
centimeters in radius from its center to the tip 
of an arm [1,3]. The dorsal color of P. aurorae 
ranges from brick with dark red markings to 
beige with brick bands along the arms and on 
the disc; the ventral color is pale yellow, with 
dark red interradial bands that reach the oral 
region [1,2]. 


References: 1: Equinodermos Antarticos. II. Asteroideos. 5. Asteroideos de la Extremidad Norte de la Peninsula Antartica. I Bernasconi. 
Revista del Museo Argentino de Ciencias Naturales "Bernardino Rivadavia" e Instituto Nacional de Investigacion de las Ciencias 
Naturales. Zoologia (aka Ciencias Zoologicas) 9(10):211-281 and plates, 1970; 2: Isidro Bosch, personal communication, 1999; 3: AM 
Clark. B.A.N.Z. Antarctic Research Expedition 1929-1931. Reports, Series B (Zoology and Botany) Volume 9, Asteroidea. Adelaide: 
BANZAR Expedition Committee, 1962; 4: Discovery Reports 20:69-306 and plates, 1940; 5: Tethys 6(3):63 1-653, 1974 


65 


seastar Perknaster fuscus 


_ 


Perknaster fuscus is found throughout Antarctica south of sixty degrees, in depths of 0 to 457 meters /5,3}. 


The color of Perknaster fuscus ranges from shades of red with darker spots or stripes to a yellow or light orange 
background with red markings |7). 


Perknaster fuscus has a color morph at Turtle Rock due to its diet of urchins and Odontaster validus seastars {6}. 


66 


Perknaster fuscus has been collected at sizes up to fourteen centimeters in radius from its center to the tip of an arm 
[7] 


67 


GAdam G Marsh 


A small Perknaster fuscus is shown here, 
with a radius of four centimeters [10]. 


68 


S 
C 
® 
= 
S 
= 
© 


69 


@Henry Kaiser / NSF 


70 


71 


Juvenile Perknaster fuscus are important predators of the sponge Homaxinella balfourensis (shown here) and also eat 
the sponges Tetilla leptoderma, Haliclona scotti, Mycale (Oxymycale) acerata, Polymastia invaginata, and 
Kirkpatrickia variolosa {1,2}. 


@Nerbert 


Here the sea urchin Sterechinus neumayeri is crawling across an adult Perknaster fuscus. Adult Perknaster fuscus 
are food-specific predators of the sponges Tetilla leptoderma, Anoxycalyx (Scolymastra) joubini, and Mycale 
(Oxymycale) acerata {2,3}. 


pee 


A juvenile Perknaster fuscus is below three Odontaster validus seastars, all eating the bush sponge Homaxinella 
balfourensis. 


‘S 


a 


~*~ 


y 


@Norbert Wu 


Perknaster fuscus can be an opportunistic scavenger on dead material [5]. Here P. fuscus is scavenging on 
something with the proboscis worm Parborlasia corrugatus. 


a 


A juvenile Perknaster fuscus eating the bush sponge Homaxinella balfourensis. 


Perknaster fuscus is eaten by the anemone Urticinopsis antarcticus 4). P. fuscus appears to be chemically defended 
from most predators |9}. 


7 


About the Perknaster seastar in the above photo, Paul Dayton said “I mentioned a white (Perknaster) eating O. 
validus (seastar) and urchins at Turtle Rock and points north ... I transplanted them to see if they would switch prey. 
Here is a photo ...that is proof that the white with pink patches did switch and eat Mycale...." (12). 


78 


@Shawn: Aer per 


TAXONOMIC NOTE: World Register of Marine Species lists a Perknaster fuscus antarcticus subspecies as an 
alternate representation (an accepted name though slightly less preferred) of Perknaster fuscus, stating “maintained 
as subspecies of Perknaster fuscus Sladen, 1889 by Bernasconi (1967) without reference to A.M. Clark (1962)” [11). 


79 


References: 1: Science 245:1484-1486, 1989; 2: Ecological Monographs 44(1):105-128, 1974 (P. Dayton, personal communication, 2015: Haliclona dancoi observations are 
corrected to H. scotti); 3: Biologie des Spongiaires, Sponge Biology. C Levi and N Boury-Esnault, eds. Colloques Internationaux du Centre National de la Recherche 
Scientifique Number 291. Paris: Centre National de la Recherche Scientifique, 1979. pp.271-282; 4: Antarctic Ecology, Volume 1. MW Holdgate, ed. NY: Academic Press, 
1970. pp244-258; 5: Adaptations within Antarctic Ecosystems: Proceedings of the Third SCAR Symposium on Antarctic Biology. George A. Llano, ed. Washington: 
Smithsonian Institution; Houston, Tex.: distributed by Gulf Pub. Co., 1977. pp.293-326; 6: P Dayton, personal communication, 1998; 7: The Fauna of the Ross Sea, Part 3, 
Asteroidea. HES Clark. New Zealand Department of Scientific and Industrial Research Bulletin 151, New Zealand Oceanographic Institute Memoir 21, 1963; 8: Tethys 
6(3):63 1-653, 1974; 9: Antarctic Ecosystems: Models for Wider Ecological Understanding. W Davison, C Howard-Williams, P Broady, eds. Christchurch, NZ: New Zealand 
Natural Sciences, 2000. pp. 158-164; 10: Paul Cziko, personal communication, 2004; 11: Mah, C.L. (2023). World Asteroidea Database. Perknaster fuscus antarcticus 
(Koehler, 1906). Accessed through: World Register of Marine Species at: www.marinespecies.org/aphia.php?p=taxdetails&id=172754 on 2023-10-27; 12: Paul Dayton, 
personal communication, 2023 


seastar Glabraster antarctica 


Gepewl Mareen 
’ - : 


<p 


? 


Glabraster antarctica is found in Antarctica and South Shetland Islands, South Sandwich Islands, South Georgia 
Island, Shag Rocks, Bouvet Island, Burdwood Bank, Falkland Islands, Chile, Uruguay, Argentina, Crozet Islands, 
Kerguelen Islands, Marion and Prince Edward Islands, Marquarie Island, and Heard Island, from 0 to 3,200 meters 
depth [3,4,6,8,9,10,13,14,15,16,17,19]. . 


Glabraster antarctica has been collected at sizes up to 9.7 centimeters in radius from its center to the tip of an arm 
[5,9,14]. 


81 


Ciewoaee- Rogelh: 


Glabraster antarctica varies in coloration as shown here. The color of G. antarctica can include off white, deep 
scarlet, pink, red purple, brick red, reddish orange, dark orange, bluish white, purplish white, bluish-grey, yellowish 
white, grey, pale orange, pale red and has also been described as various tints of dark red [6,8,9,10,13,15). 


82 


Pe 
: 
ie 
i 
S 
ee 
es 
het 
es 
es 


Glabraster antarctica is a ciliary-mucous feeder consuming the small organisms, diatoms, and detritus that shower 
down on its back by passing them along to its mouth 11,2). Glabraster antarctica occasionally is an active predator 
on larger prey and is a scavenger [2]. 


84 


Glabraster antarctica is a morphologically variable species with morphotypes that are not genetically distinct [1). 
The Antarctic Peninsula morphotype is small, with strong abactinal spination, while the large Scotia Arc 
morphotype lacks abactinal spines [13]. The Magellanic morphotype is bright red-orange with distinct abactinal 
spination [18). 


iPe 


au mn 


e % Here is a spiny form of Glabraster 

“~ oe antarctica {7,10|. Adult Glabraster 
antarctica have well developed dorsal 
spines or tubercles {1,2,4,9,10]. However 
this distinction is not so distinct in 
some specimens {4,6}. 


Taxonomic Note: Porania antarctica assigned to Glabraster genus, and subspecies glabra was synonymized {11,13}. 


References: 1: The Fauna of the Ross Sea, Part 3, Asteroidea. HES Clark. New Zealand Department of Scientific and Industrial Research Bulletin 151, New Zealand 
Oceanographic Institute Memoir 21, 1963; 2: Adaptations within Antarctic Ecosystems: Proceedings of the Third SCAR Symposium on Antarctic Biology. George A. Llano, 
ed. Washington: Smithsonian Institution; Houston, Tex. : distributed by Gulf Pub. Co., 1977. pp.293-326; 3: Los Equinodermos Colectados por el "Walther Herwig" en el 
Atlantico Sudoeste. I Bernasconi. Revista del Museo Argentino de Ciencias Naturales "Bernardino Rivadavia" e Instituto Nacional de Investigacion de las Ciencias 
Naturales. Hidrobiologia 3(3):287-334 and plates, 1973; 4: AM Clark. B.A.N.Z. Antarctic Research Expedition 1929-1931. Reports, Series B (Zoology and Botany) Volume 
9, Asteroidea. Adelaide: BANZAR Expedition Committee, 1962; 5: Biological Bulletin 177(1):77-82, 1989; 6: Discovery Reports 20:69-306 and plates, 1940; 7: Isidro 
Bosch, personal communication, 1999; 8: South African Journal of Antarctic Research 23(1-2):37-70, 1993; 9: Asteroidea with a Survey of the Asteroidea of the Chilean 
Shelf. FJ Madsen. Lunds Universitets Arsskrift. Ny Foljd, Avd. 2. Bd 52. Nr 2. Kungliga Fysiografiska Sallskapet Handlingar. Ny Foljd, Bd 67, Nr 2. Reports of the Lund 
University Chile Expedition 1948-49. Number 24. Lund: CWK Gleerup, 1956; 10: Memoirs of Museum Victoria 57(2):167-223, 1998; 11: AM Clark & ME Downey. 
Starfishes of the Atlantic. Chapman & Hall Identification Guides, 3. London: Chapman & Hall 1992; 12: W. Percy Sladen. Zoology Part 51. Report on the Asteroidea 
(Starfish) collected by H.M.S. Challenger during the years 1873-1876. Report on the Scientific Results of the Voyage of HMS Challenger during the Years 1873-76. 
Zoology, Vol 30, Text. London, HMSO: 1889. pp 360-362; 13: Zootaxa 3795(3): 327-372, 2014; 14: Fauna der Antarktis. J Sieg & JW Wagele, eds. Berlin: P Parey, 1990; 
15: Equinodermos Antarticos. II. Asteroideos. 5. Asteroideos de la Extremidad Norte de la Peninsula Antartica. I Bernasconi. Revista del Museo Argentino de Ciencias 
Naturales "Bernardino Rivadavia" e Instituto Nacional de Investigacion de las Ciencias Naturales. Zoologia (aka Ciencias Zoologicas) 9(10):211-281 and plates, 1970; 16: 
Polar Biology 41:2423-2433, 2018; 17: Amazing Antarctic asteroids: a guide to the starfish of the Ross Sea. Kate Neill et al. NIWA, New Zealand, Version 1, 2016 
www.niwa.co.nz/coasts-and-oceans/marine-identification-guides-and-fact-sheets/amazing-antarctic-asteroids; 18: Ecology and Evolution 8(21):10621-10633, 2018; 19: 
Frontiers in Ecology and Evolution 12:1455329, 2024. doi: 10.3389/fevo.2024.1455329 


85 


seastar Psilaster charcoti 


© Jim Mastro 


Psilaster charcoti is found throughout Antarctica and the Antarctic Peninsula, South Shetland Islands, South Orkney Islands, South 
Sandwich Islands, South Georgia Island, Bouvet Island, Crozet Islands, Macquarie Island, Argentina, and Chile, from 10 to 3,900 meters 
depth [1,3,4,5,6,7). The dorsal surface of P. charcoti is slightly convex; its arms are wide at the base, have steeply vertical sides, and taper 
evenly from its broad disc to the sharp arm tips [1,4). P. charcoti has a central anus, long slender tube feet without distinct sucking discs, 
and its oval madreporite is between arms and nearer the edge than center /1;. The lack of distinct suckers on the tube feet of P. charcoti 
indicates a preference for a muddy environment ,1). P. charcoti has been collected at sizes up to sixteen centimeters in radius from its 
center to the tip of an arm (2,4). The color of P. charcoti is reddish brown, brown-yellow, light tan, bright or pale pink, purplish, or violet 
and its edges may be lighter; young may be pale yellow {1,4,6). Psilaster charcoti has been collected with its stomach filled with mud, fecal 
material, the remains of a polychaete worm, and pieces of a colonial ascidian; it has also been captured with hooks baited with fish chunks 
3). Thus P. charcoti is an active predator on some invertebrates and ingests mud to eat organisms therein; it also scavenges on feces and 
dead organisms ,3}. P. charcoti is noted as being slimy, suggesting ciliary-mucus feeding ;3}. 


References: 1: The Fauna of the Ross Sea, Part 3, Asteroidea. HES Clark. New Zealand Department of Scientific and Industrial Research Bulletin 151, New Zealand 
Oceanographic Institute Memoir 21, 1963; 2: Bulletin de l'Institut Royal des Sciences Naturelles de Belgique, Biologie 63:175-184, 1993; 3: Adaptations within Antarctic 
Ecosystems: Proceedings of the Third SCAR Symposium on Antarctic Biology. George A. Llano, ed. Washington: Smithsonian Institution; Houston, Tex.: distributed by 
Gulf Pub. Co., 1977. pp.293-326; 4: Equinodermos Antarticos. II. Asteroideos. 5. Asteroideos de la Extremidad Norte de la Peninsula Antartica. I Bernasconi. Revista del 
Museo Argentino de Ciencias Naturales "Bernardino Rivadavia" e Instituto Nacional de Investigacion de las Ciencias Naturales. Zoologia (aka Ciencias Zoologicas) 
9(10):211-281 and plates, 1970; 5: Tethys 6(3):631-653, 1974; 6: Memoirs of Museum Victoria 57(2):167-223, 1998; 7: Amazing Antarctic asteroids: a guide to the starfish 
of the Ross Sea. Kate Neill et al. NIWA, New Zealand, Version 1, 2016 www.niwa.co.nz/coasts-and-oceans/marine-identification-guides-and-fact-sheets/amazing-antarctic- 
asteroids 


86 


© Rob Robbins 


possibly the seastar 
Pteraster affinis 


This seastar was photographed at New 
Harbor at about twelve meters depth (2). 


Taxonomic Note: Pteraster affinis reported by AM Clark 1). John Pearse said this photo looked like the aculeatus 
subspecies 3). That subspecies has been synonymized into the affinis parent species [4]. Genetic analysis suggests 
that Pteraster affinis should have several species [5]. An identification key to the Southern Ocean Pterasteridae is at 
pterasteridae-so.identificationkey.org/mkey.html [accessed 10 November 2021]. 


References: 1: AM Clark. B.A.N.Z. Antarctic Research Expedition 1929-1931. Reports, Series B (Zoology and Botany) Volume 9, 
Asteroidea. Adelaide: BANZAR Expedition Committee, 1962; 2: Rob Robbins, personal communication, 2000; 3: John Pearse, personal 
communication, 2000; 4: Mah, C. (2014). Pteraster affinis Smith, 1876. In: Mah, C.L. (2014) World Asteroidea database. Accessed 
through: World Register of Marine Species at www.marinespecies.org/aphia.php?p=taxdetails&id=172780 on 2014-09-03; 5: Zoological 
Journal of the Linnean Society 192(1):105-116, 2021 


87 


heart urchin Abatus sp. 


@). Da ay 


_ 


-, 


Species of Abatus urchins reported in the 
McMurdo Sound area are ingens, nimrodi, 
and shackletoni [15]. Species of Abatus 
urchins reported in Terra Nova Bay of the 
Ross Sea are ingens, nimrodi, shackletoni, 
_ agassizii, cavernosus, cordatus, curvidens, 
and elongatus [16]. 


Urchins of the genus Abatus are 
characterized by what's called a 
peripetalous fasciole in adult urchin tests 
(shells); this is a different-looking band of 
fine densely-packed spines circum- 

4, navigating the top of the test (see it below 
this red line) 115). 


88 


A live Abatus urchin showing its peripetalous fasciole, a band of fine densely-packed spines circum-navigating the 
top. 


ae tin ae ae 


Heart urchins are deposit feeders, using their oral tube feet to gather up detritus (13). Heart urchins have a dense coat 
of spines which keeps sediment away from the urchin's surface, thus maintaining a water-filled surrounding space 
that the urchin uses for respiration while buried [13}. 


90 


An Abatus sp. urchin. 


An Abatus sp. urchin. 


m4 


+ 


Me 


91 


Abatus shackletoni is found throughout Antarctica and the Antarctic Peninsula from 8 to 631 meters depth 
[1,2,3,4,9,10,12,14,15]. Near Cape Evans, Abatus shackletoni occurs in loose gravel and cobble habitats [1). At Rocher 
Jacobsen in the Pointe Géologie Archipelago of Terre Adélie, Abatus shackletoni individuals live completely buried 
in the silty sediment [14]. The shell (test) length of Abatus shackletoni can be up to 6.7 centimeters in length, with a 
typical size being four centimeters [6,11,15]. The test of Abatus shackletoni is more or less ovoid, about as long as it is 
broad, has a regular peripetalous fasciole, and may or may not have a faint notch at the anterior end [4,5,9,10,15). The 
color of Abatus shackletoni is brown to grayish-purple (15). 


Abatus (Pseudabatus) nimrodi is found in eastern Antarctica from 2 to 716 meters depth [1,4,5,6,9,14]. Abatus 
(Pseudabatus) nimrodi can be found partly or completely burrowed into muddy or silty sediment [7,14]. Abatus 
(Pseudabatus) nimrodi is common along the western oligotrophic side of McMurdo Sound including New Harbor; 
it can be found buried just below the surface of fine, silty sediment at New Harbor [1,6.9). The shell (test) length of 
Abatus (Pseudabatus) nimrodi can be up to six centimeters with an average size of 3 - 4 centimeters [15]. The brood 
pouches of Abatus (Pseudabatus) nimrodi are widely separated from the apical system at the top of the test (shell) 
(15]. The color of Abatus (Pseudabatus) nimrodi is dark brown to nearly black (4,15). 


Abatus ingens has been found along the Antarctic coast from 20 to 761 meters depth, and is very large, up to six to 
seven centimeters in length (15). Abatus ingens has a triangular-looking ambitus at its posterior end, has a sinuous- 
looking peripetalous fasciole, and is very dark, almost black, including its spines (15). 


Here's a look at the four brood pouches on 
an Abatus test (shell). 


Abatus shackletoni broods an average of 22 
yolk-feeding embryos and juveniles in each 
of four depressed elongated brood pouches 
on the urchin's dorsal (aboral) surface; 
Abatus (Pseudabatus) nimrodi broods an 
average of eighteen [1,6}. 


92 


Here, Abatus embryos and juveniles are 
pulled out of their brood pouches for 
illustration. Development of embryos 
within the brood pouch takes at least 
eight months |). Eggs are released into 
the brood pouches and fertilized there 

» throughout most or all of the year {6). 
From August to January, 71-100% of 
Abatus shackletoni females are brooding 
embryos {6}. From November to January, 
60-84% of Abatus (Pseudabatus) 
nimrodi females are brooding embryos 


[6]. 


Two types of spines form a protective 
arch over the Abatus brood pouch 11,6}. 


stages of development in the brood 
] pouch and are larger in size relative to 
» the juveniles of Abatus shackletoni (1,6}. 


93 


The production of large, 

| robust Abatus (Pseudabatus) 
nimrodi juveniles may 
increase their survival for 
escaping the predatory brittle 
stars which occur in their 
environment; these brittle 
stars are not abundant where 
Abatus shackletoni is found 


[6]. 


The diversity of Antarctic sea urchins with its prevalence of brooding (thirty-nine of sixty Antarctic and 
subantarctic species -- 65%) may be a process of species-level selection via extinction and speciation rates related 
to pelagic or protected development of their young [7,8). 


Taxonomic Note: Genetic analysis showed Abatus koehleri to be A. shackletoni {16}. 
Abatus ingens, nimrodi, shackletoni, agassizii, cavernosus, cordatus, curvidens, and elongatus were reverse 
described after genetic analyses [16}. 


References: 1: Journal of Morphology 216(1):79-93, 1993; 2: Symposium on Antarctic Oceanography. Santiago, Chile 13-16 September 1966. Published by Scott Polar 
Research Institute for Scientific Committee on Antarctic Research. Cambridge, Printed by W. Heffer, 1966. p.162; 3: R Koehler. Echinodermata Echinoidea. Australasian 
Antarctic Expedition 1911-1914. Scientific Reports. Series C, Zoology and Botany. Vol 8 Part 3. Sydney: David Harold Paisley, Government Printer, 1926; 4: A Monograph 
of the Echinoidea. Volume 2, Spatangoida. 2. Amphisternata. 2. Spatangidae, Loveniidae, Pericosmidae, Schizasteridae, Brissidae. T Mortensen. Copenhagen: CA Reitzel, 
1951. pp.249-263; 5: Hawaiian and Other Pacific Echini. The Spatangina. HL Clark. Memoirs of the Museum of Comparative Zoology at Harvard College. Volume 46 
Number 2. Cambridge: Museum of Comparative Zoology at Harvard College, 1917. pp. 174-177; 6: Invertebrate Reproduction and Development 17(3):181-191, 1990; 7: 
Vie et Milieu 47(4):38 1-387, 1997; 8: Evolution 50(2):820-830, 1996; 9: Echinoderms Through Time: Proceedings of the Eighth International Echinoderm Conference, 
Dijon, France, 6-10 September 1993. B David et al, eds. Rotterdam; Brookfield, Vt.: Balkema, 1994. pp.749-756; 10: Equinodermos Antarticos. I. Equinoideos. 1. 
Equinoideos de Shetland del Sur y Archipielago Melchior. I Bernasconi. Revista del Museo Argentino de Ciencias Naturales "Bernardino Rivadavia" e Instituto Nacional de 
Investigacion de las Ciencias Naturales. Zoologia 9(9):197-210 and plates, 1969; 11: Biogeografia de la Peninsula Antartica, Archipielagos y Mares Adyacentes. N Bellisio 
& A Tomo. Buenos Aires: Servicio de Hidrografia Naval, 1974; 12: A Survey of the Marine Fauna in Shallow Coastal Waters of the Vestfold Hills and Rauer Islands, 
Antarctica. MJ Tucker & HR Burton. ANARE Research Notes 55, 1987; 13: www.nhm.ac.uk/palaeontology/echinoids/; 14: Polar Biology 27(3):177-182, 2004; 15: 
Antarctic Echinoidea. B David, T Chone, R Mooi & C De Ridder. Ruggell, Liechtenstein: ARG Gantner, 2005; 16: Diversity 15: 875, 2023 doi.org/10.3390/d15070875 


94 


pencil urchin Ctenocidaris perrieri 


Ctenocidaris perrieri is found in Antarctica and the Antarctic Peninsula, Kerguelen Island, Crozet Island, and 
Heard Island from 6 to 602 meters depth [1,2,5,6,7). 


95 


The test (shell) of Ctenocidaris perrieri has been measured at sizes up to 6.7 centimeters and is purple or purple- 
brown in color [7,8,9}. 


Ctenocidaris perrieri has long, slender, coarsely thorny primary spines measured at lengths up to 8.5 centimeters 
and covered with a thick, spongy coat of hairs |2}. The primary spines of C. perrieri are typically twice as long as 
the horizontal diameter of the test (shell) 2}. 


Eleven sponge species were found to grow on the spines of Ctenocidaris perrieri, with the most common being 
Homaxinella balfourensis, Isodictya erinacea, Iophon unicorne, and Haliclona (Rhizoniera) dancoi; the urchins 
increase the dispersal of the sponges by being “islands” of suitable habitat ,10). 


©Shawn, Sessa 


AV j 


. \ e “5 \% 


Ctenocidaris perrieri broods its embryos and juveniles in the region surrounding its mouth (the peristome) [3,3). 


98 


©Shawn Harper 


The diversity of Antarctic sea urchins with its prevalence of brooding (thirty-nine of sixty Antarctic and subantarctic species 
-- 65%) may be a process of species-level selection via extinction and speciation rates related to pelagic or protected 
development of their young ;3,4}. 


References: 1: Bulletin du Museum National d'Histoire Naturelle, Section A, Zoologie, Biologie, et Ecologie Animales 14(2):405-441, 1992; 2: A Monograph of the 
Echinoidea. Volume 1, Cidaroidea. T Mortensen. Copenhagen: CA Reitzel, 1928. pp123-124; 3: Evolution 50(2):820-830, 1996; 4: Vie et Milieu 47(4):381-387, 1997; 5: 
NZOI Records (New Zealand Oceanographic Institute) 3(1):1-6, 1976; 6: Jim Mastro, personal communication, 1999 [6 meters at Explorer's Cove in New Harbor]; 7: 
Equinodermos Antarticos. I. Equinoideos. 1. Equinoideos de Shetland del Sur y Archipielago Melchior. I Bernasconi. Revista del Museo Argentino de Ciencias Naturales 
"Bernardino Rivadavia" e Instituto Nacional de Investigacion de las Ciencias Naturales. Zoologia 9(9):197-210 and plates, 1969; 8: T Mortensen. B.A.N.Z. Antarctic 
Research Expedition 1929-1931. Reports, Series B (Zoology and Botany) Volume 4, Part 10 Echinoidea. pp. 287-310 plus plates. Adelaide: BANZAR Expedition 
Committee, 1950; 9: Echinodermes (Asteries, Ophiures et Echinides). R Koehler. Deuxieme Expedition Antarctique Francaise (1908-1910) commandee par le Dr Jean 
Charcot. Sciences Naturelles. Documents Scientifiques. Paris: Masson et Cie, 1912; 10: Polar Biology 32(7):1067-1076, 2009 


99 


sea urchin Sterechinus neumayeri 


Sterechinus neumayeri is found in Antarctica and the Antarctic Peninsula, South Shetland Islands, South Orkney 
Islands, South Sandwich Islands, South Georgia Island, South Patagonia Island, Prince Edward Island, Marion 
Island, Crozet Island, and Kerguelen Island at depths from 5 to 640 meters [s,9,10). 


Sterechinus neumayeri is abundant in shallow waters of McMurdo Sound at depths less than fifteen meters and 
plays a major role in McMurdo Sound's benthic ecosystem. 


101 


102 


O©Norbert Wu 


The color of the test (shell) and spines of Sterechinus neumayeri is variable, from greenish- olive to dark 
purplish/violet or whitish; the test is more generally greenish-olive or green-gray [8,9,10]. It is slow growing, reaching 
a maximum diameter of seven centimeters at forty years of age [1). 


The bare test (shell) of the genus Sterechinus is distinguished by a large periproct within its ring of apical plates, 
distinctly darker lines formed by tube feet in the pore zones, and denser distribution of tubercules on the oral side 
than the aboral side 119] 


103 


ONS ge Shaaw 


Largely herbivorous, half of the diet of Sterechinus neumayeri is algae; it also eats diatoms, foraminiferans, 
sponges, bryozoans, hydrozoans, polychaetes including Spirorbis sp., and amphipods (4,18,20}. 


104 


©Nerbert Wu 


Above, Sterechinus neumayeri and the seastar Odontaster validus cruise the shallow bottom foraging for food 
around the crystalline anchor ice. 


105 


Weddell seal feces are a food item for Sterechinus neumayeri in shallow water, which can be observed piled up on 
feces along with the seastar Odontaster validus. The gut content of S. neumayeri is filled with seal feces at locations 
where this occurs {5}. 


Sterechinus neumayeri has been observed feeding on the detrital film on the surface of the sponge Cinachyra 
antarctica [13]. 


Like many other urchins, 
Sterechinus neumayeri attaches bits 
of shell and debris to itself. The 
shells and debris often have stinging 
hydroids on them (see the whitish 
polyps on top left of the urchin). If an 
anemone like Urticinopsis 
antarcticus touches the urchin's 
hydroids, it releases the urchin. If 
the urchin is aware of the anemone's 
tentacles, the urchin releases its 
protective camouflage and escapes 
the anemone's grasp. If this 
camouflage isn't present on the 
urchin, the anemone captures and 
eats the urchin (3). 


Predators of the urchin Sterechinus neumayeri include the anemones Urticinopsis antarcticus and Isotealia 
antarctica, the octopus Pareledone sp., the fish Trematomus bernacchii, the seastars Macroptychaster accrescens 
and Odontaster validus [shown here], and the brittle star Ophiosparte gigas [6,7,11,12,14,16]. 


108 


Sterechinus neumayeri attaches pieces of 
algae like Phyllophora antarctica and Iridaea 
cordata to itself as protection against the 
anemone /sotealia antarctica (14). 


Both algae manufacture unpalatable defensive 
chemicals to avoid getting eaten by 
Sterechinus. neumayeri, yet the urchin 
attaches algal pieces to itself as a detachable 
shield to shed when the anemone's tentacles 
grab onto the attached algae (14,15). 


The Antarctic scallop Adamussium colbecki may be colonized on either shell by small hydroids Hydractinia 
angusta 7. H. angusta hydroids eat tube feet and pedicellariae of sea urchins including Sterechinus neumayeri, 
which graze on the algal film growing on the surface of the scallop's shell but is not a predator of the scallop in. 
Adamussium colbecki shells are very thin, and such urchin grazing may damage the shell; thus the hydroids act in 
defense of the scallop 11. 


110 


At some sites where these algae occur with Sterechinus neumayeri, 96.5% of the urchins were using Phyllophora 
antarctica for 90% or more of their cover [14). This is a mutually beneficial relationship between S. neumayeri and 
the algae 14}. The urchins move fertile drift algae throughout sunlit waters, thereby keeping drift algae in the 
reproductive area with other attached and drift algae; the urchins also extend the vertical and horizontal range of the 
algae and facilitate recolonization after ice scouring of the bottom or when conditions allow growth of attached 
plants at greater depths (14). 


111 


and 
\ 


Jr) 


‘~ 


Spawning Sterechinus neumayeri 


Sterechinus neumayeri spawning is timed so 
that its feeding larvae are in the plankton during 
the short summer peak of phytoplankton 
abundance [2}. 


References: 1: Marine Biology 124(2):279-292, 1995; 2: Biological Bulletin 173(1):126-135, 1987; 3: Antarctic Ecology, Volume 1. MW Holdgate, ed. NY: Academic 
Press, 1970. pp.244-258; 4: Antarctic Journal of the United States 11(1):24-26, 1976; 5: Biological Bulletin 130(3):387-401, 1966; 6: Polar Biology 13(5):347-354, 1993; 7: 
Ecological Monographs 44(1):105-128, 1974; 8: A Monograph of the Echinoidea. Volume 3, Part 3. Camarodonta 2. Echinidae, Strongylocentrotidae, Parasaleniidae, 
Echinometridae. T Mortensen. Copenhagen: CA Reitzel, 1943. pp.106-108; 9: Bulletin du Museum National d'Histoire Naturelle, Section A, Zoologie, Biologie, et Ecologie 
Animales 14(2):405-441, 1992; 10: Equinodermos Antarticos. I. Equinoideos. 1. Equinoideos de Shetland del Sur y Archipielago Melchior. I Bernasconi. Revista del Museo 
Argentino de Ciencias Naturales "Bernardino Rivadavia" e Instituto Nacional de Investigacion de las Ciencias Naturales. Zoologia 9(9):197-210 and plates, 1969; 11: 
Bulletin de l'Institut Oceanographique 66(1368), 1966; 12: Adaptations within Antarctic Ecosystems: Proceedings of the Third SCAR Symposium on Antarctic Biology. GA 
Llano, ed. Washington: Smithsonian Institution; Houston, TX : distributed by Gulf Pub. Co., 1977. pp.293-326; 13: New Zealand Antarctic Record 9(2):34-52, 1989; 14: 
Marine Ecology Progress Series 183:105-114, 1999; 15: Journal of Phycology 34(1):53-59, 1998; 16: Polar Biology 16(5):309-320, 1996; 17: Polar Biology 23(7):488-494, 
2000; 18: Polar Biology 26(2):99-104, 2003; 19: Sea Urchins, a Guide to Worldwide Shallow Water Species. H Schultz. Hemdingen, Germany: Heinke & Peter Schultz 
Partner Scientific Publications, 2006; 20: Nature Scientific Reports 14:12333, 2024 doi.org/10.1038/s41598-024-62644-5 


112 


brittle star Astrotoma agassizii 


Astrotoma agassizii occurs throughout Antarctica and the Antarctic Peninsula, South Shetland Islands, South 
Georgia Island, Shag Rocks, Falkland Islands, Burdwood Bank, and southern Chile and Argentina, in depths from 
55 to 1,335 meters [1,2,3,4,8,9]. 


@®Paul>y @ziko 


Astrotoma agassizii is creamy white in color (2). The central disk of A. agassizii can reach a diameter of six 
centimeters (2,6). From its growth rings, maximum age of A. agassizii is estimated to be 91 years [7}. A. agassizii 
bears live young and is hermaphrodite ,3). 


114 


The unbranched arms of Astrotoma agassizii are 
stout, tapering, and flexible, reaching a length of 
seventy centimeters [2,6]. 


Astrotoma agassizii is usually found on sponges 
(as shown here on Anoxycalyx (Scolymastra) joubini), 
corals, and other organisms on which it can climb 
to be more advantageously placed to feed on prey 
drifting by [1,2]. The stomach of A. agassizii 
contains diatoms, phytoplankton, foraminiferans, 
chaetognaths, bryozoans, polychaetes, 


holothurians, ascidians, and primarily crustaceans 
(including mysids, copepods particularly Euchaeta 
antarctica and Calanoides acutus, euphausiids, and 


amphipods, ostracods), indicating that it feeds on 
plankton, catching them with its flexible long 
arms, which are armed with hooks and spines to 
increase catch efficiency [1,2,5,6,71. One or two arms 
cling to the perch, while the others extend to feed 
[6]. The arms of A. agassizii can be looped and twisted, increasing its efficiency at contacting prey [1). Prey caught by 
the arm tips of A. agassizii are rolled up into coils and passed to the mouth 11). 


Taxonomic Note: Astrotoma agassizii may be a species complex; Clade I is distributed across the Antarctic 
continental shelf and South Georgia and is genetically discrete with dispersing pelagic larva {10}. Reproductive 
incompatibility in this species complex was not shown in this work: “Speciation involves the evolution of 
reproductive incompatibilities between diverging populations, including prezygotic incompatibilities that prevent 
the formation of hybrids and postzygotic incompatibilities that render hybrids sterile or inviable [11).” A “periodic- 
like morphological and molecular framework” applied to the Cadlina nudibranch genus in the Kuril Islands showed 
the term “cryptic species” should be removed from phylogeny and taxonomy, and that different species of this 
complex varied in molecular phylogenetic distances and morphological distinctness [1}. 


References: 1: Adaptations within Antarctic Ecosystems, Proceedings of the Third SCAR Symposium on Antarctic Biology. GA Llano, 
ed. Washington, DC: Smithsonian Institution, 1977. pp.293-326; 2: The Fauna of the Ross Sea, Part 1, Ophiuroidea. HB Fell. New 
Zealand Department of Scientific and Industrial Research Bulletin 142, New Zealand Oceanographic Institute Memoir 18, 1961; 3: Physis 
25(69):2-5, 1965; 4: US National Museum Polar Invertebrate Catalog at www.nmnh.si.edu/iz/usap/usapdb.html; 5: Journal of Plankton Research 
11(6):1315-1320, 1989; 6: Antarctic Research Series 44:1-28, 1986. Biology of the Antarctic Seas, Volume 17. Washington: American 
Geophysical Union, 1986; 7: Berichte zur Polarforschung 194, 1996; 8: Boletim do Instituto Oceanografico (Sao Paulo) 32(1):33-54, 
1983; 9: Polar Biology 38:799-813, 2015; 10: Heredity 123:622-633, 2019; 11: eLife 7:e35468. doi.org/10.7554/eLife.35468; 12: 
Diversity 2024, 16, 220 doi.org/10.3390/d16040220 


115 


brittle star Ophiacantha antarctica 


is, 
2h ss | 
» < wears 


© Norbert Wu o: 


Ophiacantha antarctica is found throughout Antarctica and the Antarctic Peninsula, South Shetland Islands, South 
Georgia Island, Bouvet Island, and the Antarctic Ocean south of the polar circle in depths from 20 to 3,398 meters 
[1,2,4,5,6,7]. 


116 


©Norbert Wu 


The color of Ophiacantha antarctica is variable including disc colors of bluish-grey, grey, reddish, and purple and 
arm colors of orange, straw, and pinkish [2,3). 


117 


/ 


. Fe 
4i¢ | [ MP 


The pentagonal central disc of Ophiacantha antarctica is up to 1.3 centimeters in diameter with indentations on the 
sides between arms [2.4]. The slender, fragile arms of O. antarctica are up to nine centimeters in length [2,4]. 


118 


COnarbert wt 


Ophiacantha antarctica is generally found up on the substrate (rocks, sponges, sessile cnidarians, etc.) [1,3]. 


Ophiacantha antarctica is an active forager and its diet includes diatoms, foraminifera, copepods, and other 
microzooplankton [1). 


119 


Its flexible arms, long erect and thin arm spines, and climbing ability suggests that Ophiacantha Antarctica feeds 
by manipulating its arms and arm spines to capture its food on or near the bottom (1). 


Ophiacantha antarctica is the most abundant and widely distributed echinoderm in the Ross Sea, playing an 
important role in the benthic biological balance (2). 


References: 1: Adaptations within Antarctic Ecosystems: Proceedings of the Third SCAR Symposium on Antarctic Biology. George A. 
Llano, ed. Washington: Smithsonian Institution; Houston, Tex.: distributed by Gulf Pub. Co., 1977. pp.293-326; 2: The Fauna of the Ross 
Sea, Part 1, Ophiuroidea. HB Fell. New Zealand Department of Scientific and Industrial Research Bulletin 142, New Zealand 
Oceanographic Institute Memoir 18, 1961; 3: John Dearborn, personal communication, 1999; 4: Equinodermos Antarticos. III. 
Ofiuroideos. 1. Ofiuroidoes del Extremo Norte de la Peninsula Antartica. I Bernasconi and MM D'Agostino. Revista del Museo Argentino 
de Ciencias Naturales "Bernardino Rivadavia" e Instituto Nacional de Investigacion de las Ciencias Naturales. Hidrobiologia 4(2):81-133 
and plates, 1974; 5: Tethys 6(3):63 1-653, 1974; 6: Polar Biology 26(11):691-699, 2003; 7: Polar Biology 38:799-813, 2015 


120 


brittle star Ophionotus victoriae 


Ophionotus victoriae occurs throughout Antarctica and the Antarctic Peninsula, South Shetland Islands, South 
Sandwich Islands, South Georgia Island, and Bouvet Island in depths from 5 to 1,266 meters [3,4,5,6). 


121 


The arms of Ophionotus victoriae are short, flattened, robust, and depressed, taper rapidly, and can reach a length 
of nine centimeters (3). 


122 


CNGmbert Wu 


re 


Osha aCe 


Ophionotus 
victoriae 
uses its two 
leading arms 


| ina typical 
> brittle star 


rowing 
fashion as it 


* moves on the 


seafloor 
searching for 
food [2}. 


* 
ys". 
<< uhh bite eee 


124 
The central disk of Ophionotus victoriae is large, flat and circular and can reach a diameter of four centimeters (3). 


Ophionotus victoriae 1s variable in color, including brown, red-brown, brick-red, yellowish-pink, bluish grey, grey, 
white, brownish- violet with darker patches, grey with radial fawn streaks, and brownish-grey; pinkish-fawn banded 
arms have been observed [3,5]. 


©Shawn Harper 


The maximum age of Ophionotus victoriae has been estimated at 22 years [9}. 


Ophionotus victoriaeis a broadcast spawner [10]. 


126 


Ophionotus 
victoriae is an 
opportunistic 
predator and also a 
scavenger and 


' detrital feeder [2]. O. 


victoriae has a 
varied diet 
including seal feces, 
diatoms, 
foraminiferans, 
tunicates/ascidians, 
sponges, hydroids, 
bryozoans, 
polychaetes, bivalve 
molluscs, 
crustaceans 
(euphausiid krill, 
copepods, amphipods, 
mysids), Sea urchins, 
and brittle stars 
[1,2,9]. 


Ophionotus 


victoriae is a significant predator of brittle stars including its own species (cannibalism), which mostly involves 


adults eating juveniles (2). 


Predators of Ophionotus victoriae include fish and the larger brittle star Ophiosparte gigas (2,71. Ophionotus 
victoriae has been observed to respond to contact by the larger brittle star Ophiosparte gigas by quickly fleeing (7.8). 
If successful in capture, Ophiosparte gigas holds the disc of Ophionotus victoriae under its own and clips off arms 
to ingest [7]. 


References: 1: 
Polar Biology 
3(3):127-139, 
1984; 2: 
Adaptations 
within Antarctic 
Ecosystems, 
Proceedings of 
the Third SCAR 
Symposium on 
Antarctic 
Biology. GA 
Llano, ed. 
Washington, 
DC: Smithsonian 
Institution, 1977. 
pp.293-326; 3: 
The Fauna of the 
Ross Sea, Part 1, 
Ophiuroidea. HB 
Fell. New 
Zealand 
Department of 
Scientific and 
Industrial 
Research 
Bulletin 142, 
New Zealand 
Oceanographic 
Institute Memoir 
18, 1961; 4: 
Fauna der 
Antarktis. J Sieg 
& JW Wagele, 
eds. Berlin: P. 
2 “i a . 7: ‘ Parey, 1990; 5: 
os 1 PPS shige Peek: : OVE: Es AFJ Madsen. 
Ra Dna Yi, Bs ke tig B.A.N.Z. 
: P Antarctic 
Research 
Expedition 
1929-1931. 
Reports, Series 
B (Zoology and 
Botany) Volume 
9, Part 3, 
Ophiuroidea. 
Adelaide: 
BANZAR 
Expedition 
Committee, 
1967; 5: 
Equinodermos 
Antarticos. III. 
Ofiuroideos. 1. 
Ofiuroidoes del 
Extremo Norte 
de la Peninsula 
Antartica. I 
Bernasconi and 
MM D'Agostino. 
Revista del 
Museo 
Argentino de 
Ciencias 
Naturales 
"Bernardino 
Rivadavia" e 
Instituto 
Nacional de 
Investigacion de 
, las Ciencias 
Naturales. Hidrobiologia 4(2):81-133 and plates, 1974; 6: Echinodermata from the Palmer Archipelago, South Shetlands, South Georgia and the Bouvet Island... . JA Grieg. 
Oslo: I Kommisjon Hos Dybwad, 1929. Scientific Results of the Norwegian Antarctic expeditions, 1927-1928 and 1928-1929 No. 2. Norske Videnskaps-Akademi i Oslo No. 
2; 7: Polar Biology 16(5):309-320, 1996; 8: Norbert Wu, personal communication, 1999; 9: Okologie und Populationsdynamik Antarktischer Ophiuroiden (Echinodermata), 
Ecology and Population Dynamics of Antarctic Ophiuroids (Echinodermata). C Dahm. Berichte zur Polarforschung, Reports on Polar Research 194, 1996; 10: Molecular 
Ecology 32(13):3382-3402, DOE 10.1111/mec.16951 


i 


129 


brittle star Ophioplinthus sp., probably Ophioplinthus gelida 


Shown here on a lacy bryozoan, this Ophioplinthus sp. is probably Ophioplinthus gelida which is the most common 
member of the genus in McMurdo Sound |3). Dorsal photos are inadequate for distinguishing O. gelida from other 
species [3]. Ophioplinthus gelida is found throughout Antarctica and the Antarctic Peninsula, South Shetland 
Islands, South Sandwich Islands, and Bouvet Island in depths from 40 to 2,725 meters (2,4,5,6.8,11). 


The pentagonal or rounded-pentagonal disc of Ophioplinthus gelida is flattened and up to 2 centimeters in diameter 
(2). The arms of O. gelida are long and tapering and reach a length of six centimeters (2,6). O. gelida is colored 
orange-brown or yellowish-brown 2}. 


ON GS bat. Wu. 


Predators of Ophioplinthus gelida include the brittle star Ophiosparte gigas {7|. The maximum age of O. gelida has 
been estimated at 33 years [9. 


Ophioplinthus gelida captures prey or feeds by moving surface sediments into small mounds which are partially or 
completely engulfed; this feeding behavior gathers small organisms as well as eggs and fecal material [1]. O. gelida 
feeds on diatoms, silicoflagellates, bryozoans, tunicates/ascidians, foraminifera, polychaetes, gastropods, 
polychaetes, sponges, bivalve molluscs, amphipods, and euphausiid krill [1,9). 


132 


Some Ophioplinthus species may be 
parasitized by an epizoic sponge Jophon 
radiatum (2). I. radiatum is dark brown, 
obscures the brittle star's true color, and 
grows on the disc and arm bases of 
Ophioplinthus (2). Presence of I. 
radiatus is not definitive for identifying 
O. gelida; some O. gelida lack it and 
other species of Ophioplinthus have it 
[2.3.5]. 


Taxonomic Note: Ophiurolepis genus was synonymized into Ophioplinthus {10}. 


References: 1: Adaptations within Antarctic Ecosystems: Proceedings of the Third SCAR Symposium on Antarctic Biology. George A. 
Llano, ed. Washington: Smithsonian Institution; Houston, Tex.: distributed by Gulf Pub. Co., 1977. pp.293-326; 2: The Fauna of the Ross 
Sea, Part 1, Ophiuroidea. HB Fell. New Zealand Department of Scientific and Industrial Research Bulletin 142, New Zealand 
Oceanographic Institute Memoir 18, 1961; 3: John Dearborn, personal communication, 1999; 4: Fauna der Antarktis. J Sieg & JW 
Wagele, eds. Berlin: P. Parey, 1990; 5: AFJ Madsen. B.A.N.Z. Antarctic Research Expedition 1929-1931. Reports, Series B (Zoology and 
Botany) Volume 9, Part 3, Ophiuroidea. Adelaide: BANZAR Expedition Committee, 1967; 6: Equinodermos Antarticos. HI. Ofiuroideos. 
1. Ofiuroidoes del Extremo Norte de la Peninsula Antartica. I Bernasconi and MM D'Agostino. Revista del Museo Argentino de Ciencias 
Naturales "Bernardino Rivadavia" e Instituto Nacional de Investigacion de las Ciencias Naturales. Hidrobiologia 4(2):81-133 and plates, 
1974; 7: Polar Biology 16(5):309-320, 1996; 8: Tethys 6(3):631-653, 1974; 9: Okologie und Populationsdynamik Antarktischer 
Ophiuroiden (Echinodermata), Ecology and Population Dynamics of Antarctic Ophiuroids (Echinodermata). C Dahm. Berichte zur 
Polarforschung, Reports on Polar Research 194, 1996; 10: Marine Biology Research 4(1-2):76-111, 2008; 11: Polar Biology 38:799-813, 
2015 


133 


brittle star Ophiosparte gigas 


Ophiosparte gigas is found throughout Antarctica and the Antarctic Peninsula at depths from 8 to 1,200 meters 
[1,2,3,4,5]. 


134 


©Norbert. wu 


The disc of Ophiosparte gigas is thick, mucus-covered, convex, and up to seven centimeters in diameter; its large 
disc relative to the arms makes it easy to recognize [1,45]. The arms of Ophiosparte gigas have spatulate arm spines, 
conical tube feet, and are up to seventeen centimeters long [1.4.5]. 


Ophiosparte gigas is colored pink, deep pink, pinkish orange, deep reddish, purplish brown, or brick red [1,4,5}. 


135 


Ophiosparte gigas lives on soft substrate; its movement is made more efficient by its paddle-like arm spines and 
stilt-like tube feet (1. 


Canadian Museéiin- S8e 


= 


4 


Ophiosparte gigas is an 
active benthic predator 
on large prey, primarily 
brittle stars (including its 
own species, 
Ophiurolepis gelida, 
Ophionotus victoriae, 
Ophiacantha sp., 
Ophiocten sp.), bivalves 
(including Adamussium 
colbecki, Aequiyoldia 
eightsti, Yoldiella 
sabrina), polychaete 
worms, crustaceans, 
and sponges [2,5]. O. 
gigas also preys on 
diatoms, algae, 
foraminifera, hydroids, 
nematodes, gastropods 
(including Nacella 
concinna), sea spiders, 
ostracods, mysids, 


amphipods, isopods, euphausiids (including Euphausia crystallorophias, Euphausia superba), the shrimp Chorismus 
antarcticus, bryozoans, cheilostomes, the crinoid Promachocrinus kerguelensis, seastars, and sea urchins (including 


Sterechinus neumayeri) (5). 


137 


eBruce A Miller 


The brittle star Ophionotus victoriae has been observed to respond to Ophiosparte gigas contact by quickly fleeing 
(5.6]. If successful in capture, Ophiosparte gigas holds the disc of Ophionotus victoriae under its own and clips off 
arms to ingest [5]. 


Ophiosparte gigas is also a scavenger [2,5]. 


References: 1: The Fauna of the Ross Sea, Part 1, Ophiuroidea. HB Fell. New Zealand Department of Scientific and Industrial Research 
Bulletin 142, New Zealand Oceanographic Institute Memoir 18, 1961; 2: Adaptations within Antarctic Ecosystems: Proceedings of the 
Third SCAR Symposium on Antarctic Biology. George A. Llano, ed. Washington: Smithsonian Institution; Houston, Tex.: distributed by 
Gulf Pub. Co., 1977. pp.293-326; 3: Jim Mastro, personal communication, 1999 [10 meters at Explorer's Cove in New Harbor]; 4: 
Equinodermos Antarticos. III. Ofiuroideos. 1. Ofiuroidoes del Extremo Norte de la Peninsula Antartica. | Bernasconi and MM D'Agostino. 
Revista del Museo Argentino de Ciencias Naturales "Bernardino Rivadavia" e Instituto Nacional de Investigacion de las Ciencias 
Naturales. Hidrobiologia 4(2):81-133 and plates, 1974; 5: Polar Biology 16(5):309-320, 1996; 6: Norbert Wu, personal communication, 
1999 


138 


sea cucumber Staurocucumis liouvillei 


Staurocucumis liouvillei has been collected in 
Antarctica and the Antarctic Peninsula and 
Bouvet Island, Heard Island and South 
Georgia Island from 60 to 791 meters depth 
(2,3,5]. S. liouvillei has been collected at sizes 
up to eight centimeters long [1,5]. 


=” Staurocucumis liouvillei lives attached to 


sponges, gorgonians (as shown here), and 
large stones [4]. 


139 


©Adam G Marsh 


Taxonomic Note: In earlier literature, it may appear under the genera Cucumaria or Abyssocucumis [1,3,5}. 
Staurocucumis liouvillei is a species complex comprising several discrete species [6]. 


References: 1: S Ekman. Holothurien. Further Zoological Results of the Swedish Antarctic Expedition 1901-1903. Volume 1, Number 6. 
Stockholm: PA Norstedt & Soner, 1925; 2: Berichte zur Polarforschung 41:1-87, 1988; 3: Tethys 5(4):601-610, 1974; 4: Polar Biology 
11(3):145-155, 1991; 5: Memoirs of Museum Victoria 59(2):297—325, 2002; 6: Polish Polar Research 34(1):67-86, 2013 


sea cucumber Staurocucumis turqueti 


Staurocucumis turqueti is found in Antarctica and the Antarctic Peninsula and South Orkney Islands from 10 to 385 
meters depth :245s S.turqueti has been collected at lengths up to thirty centimeters ,;, 


Staurocucumis turqueti is chestnut or brown colored [1,2). 


OSI Hat ees 


Staurocucumis turqueti is a suspension feeder and has been observed on the sediment surface holding the anterior 
half of its body vertically up in the water to suspension feed |S. turqueti has been observed attached to sponges («, 


Taxonomic Note: Appears under other genera in the older literature including Abyssocucumis, Cucumaria and 
Ekmocucumis (23,4,7|. Staurocucumis grandis 1s a synonym of S. turqueti {9}. 


References: 1: C Vaney. Holothuries. Expedition Antarctique Francaise (1903-1905). Paris: Masson et Cie, 1906; 2: S Ekman. 
Holothurien. Further Zoological Results of the Swedish Antarctic Expedition 1901-1903. Volume 1, Number 6. Stockholm: PA Norstedt & 
Soner, 1925; 3: Julian Gutt, personal communication, 1999; 4: Tethys 5(4):601-610, 1974; 5: Berichte zur Polarforschung 41:1-87, 1988; 
6: Polar Biology 11(3):145-155, 1991; 7: Memoirs of Museum Victoria 59(2):297—325, 2002; 8: Polar Biology 38:799-813, 2015; 9: 
Zootaxa 2016(1):1-16, 2009 


143 


sea cucumber Bathyplotes bongraini 


TeNforber tain 


Bathyplotes bongraini is found throughout Antarctica and the Antarctic Peninsula and Bouvet Island at depths from 
4.5 to 768 meters [1,3,4,5.6,7,8]. B. bongraini has been collected at lengths up to 26 centimeters [1,6). B. bongraini is 
usually colored dark pink with a distinct dark brown cross-band, two to three centimeters wide, slightly behind the 
middle of the body (11. 
tha © Jim Mastro 


The dorsal conical papillae of Bathyplotes 
bongraini are 1-5 millimeters high [1). 

B. bongraini is a sediment feeder 2]. The 
mouth of B. bongraini is turned down 
(ventrally) and its anus is subdorsal [1). 


Taxonomic Note: Older species name was fuscivinculum (6). 


References: 1: Zoologica Scripta 19(1):119-127, 1990; 2: Polar Biology 11(3):145-155, 1991; 3: Jim Mastro, personal communication 
(New Harbor 21 & 28 meters [photo]; Hutton Cliffs 4.5 meters), 1999; 4: Peter Brueggeman, personal communication (New Harbor 26 
meters), 1999; 5: Polar Biology 20(4):229-247, 1998; 6: Memoirs of Museum Victoria 59(2):297-325, 2002; 7: Polar Biology 29(2):83- 
96, 2006; 8: Polar Biology 38:799-813, 2015 


144 


sea cucumber Cucumaria spp. 


These Cucumaria spp. sea cucumbers are impossible to identify to the species level from this photo [1). Even with 
specimens on hand, identification is difficult; the literature of this group is confusing, and they have been referred 
to as Cucumaria georgiana-group [1,2]. 


Cucumaria spp. has been observed attached to sea urchins, branched bryozoans, and hydroid stalks {2}. Here 
Cucumaria spp. sea cucumber is perched on algae Phyllophora antarctica on top of the sea urchin Sterechinus 
neumayeri. 


References: 1: Julian Gutt, personal communication, 1999; 2: Polar Biology 11(3):145-155, 1991 


145 


sea cucumber Echinopsolus acanthocola 


Echinopsolus 
acanthocola has 
been collected in the 
Weddell Sea and 
Bouvet Island at 
depths from 177 to 
650 meters ,14;7. Here 
it is photographed at 
scuba diving depth in 
McMurdo Sound. E. 
acanthocola has 
scattered peaked 
cone-shaped 
processes on its body 
wall and its color is 
rose to brownish-red 
[1,6]+ 

Echinopsolus 
acanthocola is a 
suspension feeder 
and has a narrow 
sole delimited by 
tube feet, which 
restricts it to using 
narrow, rod-like 
structures as 
substrate; it has been 
collected attached to 
sea urchin spines pq). 
Here E. acanthocola 
is attached to the sea 
urchin Sterechinus 
neumayeri and it has 
been collected 
attached to the pencil 
urchin Ctenocidaris 
perrieri \3), 


Echinopsolus acanthocola has been collected at 
lengths up to 2.3 centimeters long 11,. 


147 


© Bruce A. Miller 


The species name acanthocola is 
composed of Colere (meaning "to 
inhabit") and Acantha (meaning 
"spine, thorn") to indicate that this 
sea cucumber species is well 
adapted to live on sea urchin 
spines and similar structures ,,,. 


References: 1: Zoologica Scripta 19(1): 101-117, 1990; 2: Polar Biology 11(3):145-155, 1991; 3: Bulletin de l'Institut Royal des Sciences 
Naturelles de Belgique, Biologie 62:179-191, 1992; 4: Polar Biology 29(2):106-113, 2006; 5: Polar Biology 38:799-813, 2015; 6: Zootaxa 
3841(4):573-591, 2014; 7: Zootaxa 2196:1-18, 2009 


148 


sea cucumber Heterocucumis steineni 


©Peter Brueggeman 


Heterocucumis steineni is found in Antarctica and the Antarctic Peninsula, South Shetland Islands, South Orkney 
Islands, South Georgia Island, Falkland Islands, and Burdwood Bank from 0 to 1,200 meters depth [2.3.5]. H. steineni 
is beige to chestnut brown, can be almost white or white and brown in one specimen, and has dark spots between 
tentacles [1,56]. H. steineni is up to fifteen centimeters long (2). 


149 


ONombert Wu 


Heterocucumis steineni may attach to other organisms like hydroids and fan-shaped bryozoans or it may live with 


the lower half of its body in sediment (4,7). This facultative lifestyle may explain why its posterior feet are wart-like 
and its anterior feet are exceptionally long, up to five millimeters (4,7). 


150 


© Peter Brueggeman 


Heterocucumis steineni is a suspension 
feeder [4,7]. 


Heterocucumis steineni is one of the most 
widely spread Dendrochirotida sea 
cucumbers in the Weddell Sea 14}. 


Taxonomic Note: In earlier literature, appears under different genera including Cucumaria, Ekmocucumis, and 
Heterocucumis {8}. 


References: 1: C Vaney. Holothuries. Expedition Antarctique Francaise (1903-1905). Paris: Masson et Cie, 1906; 2: S Ekman. Holothurien. Further Zoological Results of 
the Swedish Antarctic Expedition 1901-1903. Volume 1, Number 6. Stockholm: PA Norstedt & Soner, 1925; 3: Berichte zur Polarforschung 41:1-87, 1988; 4: Polar Biology 
11(3):145-155, 1991; 5: Fauna der Antarktis. J Sieg, JW Wagele, eds. Berlin: P Parey, 1990; 6: Julian Gutt, personal communication, 2000; 7: Polar Biology 11(8):533-544, 
1992; 8: Memoirs of Museum Victoria 59(2):297—325, 2002; 9: Polar Biology 38:799-813, 2015 


151 


sea cucumber, group Aspidochirotida 


Taxonomic Note: Not Staurocucumis turqueti (x. 


References: 1: Julian Gutt, personal communication, 2000 


152 


crinoid Promachocrinus kerguelensis 


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Y 
5 
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©Norbert Wy, 


Promachocrinus kerguelensis is found throughout Antarctica and the Antarctic Peninsula, South Shetland Islands, 
South Georgia Island, Bouvet Island, Kerguelen Island, and Heard Island, from 10 to 2,100 meters depth [3,4.6,9}. P. 
kerguelensis is also found in the Strait of Magellan, and between Australia/New Zealand and the Antarctic 


continent ([3,4,7]. 


153 


©Adam G. Marsh 


Promachocrinus kerguelensis has ten biradiate rays (20 arms), is the most widely distributed and abundant crinoid 


in Antarctica and subantarctic islands, is the largest comatulid (unstalked) crinoid in southern latitudes and is the 
only 20-armed comulatid crinoid in high southern latitudes [3,4,9}. 


154 


Promachocrinus kerguelensis can be solid colored or banded; its color ranges from ivory to buff with light to dark 
brown pinnules and if banded, the bands can be dark to reddish brown j3,4}. Individuals from the Ross Sea may be 
more uniform in color; solid color and banded specimens can occur in the same population [4}. 


Ihe fs) 


SN AN!’ 


- 


The arms of Promachocrinus kerguelensis are edged with feathery pinnules containing sensory tube feet and 
reproductive organs. The arms are used to trap drifting plankton and they have grooves down which food particles 
are carried by hair-like cilia to the upward-facing mouth. Its different feeding postures (a filtration fan, a radial 
posture with its pinnules in one plane, and a collecting bowl) are suggested as a response to ocean currents [3]. 


156 


Promachocrinus kerguelensis produces large numbers of buoyant eggs which spawn into the plankton in November 
and December in McMurdo Sound; it doesn't brood eggs in its arms as do some Antarctic crinoids ,1). Settlement of 


its free-floating larvae occurs 2 to 3 months later when the seasonal Antarctic plankton bloom is high and offers a 
rich food source [1}. 


Promachocrinus kerguelensis (and other comatulid crinoids) cling and move by walking on specialized curved 
structures called cirri (seen at lower left). P. kerguelensis clings to sponges, worm tubes, gorgonians, and rocks as 


well as mud and gravel |2,3}. This gives P. kerguelensis a high perch above the seafloor which may protect it from 
fish nibbling on its extended arms [2). 


158 


Promachocrinus kerguelensis is not toxic to fish, but there are no Antarctic fish living in the water above the 
seafloor to nibble at its arms ,2}. The predatory brittle star Ophiosparte gigas has been found to have P. kerguelensis 
in its gut contents [5]. 


Taxonomic Note: Genetic analysis shows that Promachocrinus kerguelensis may be comprised of two cryptic 
species [sg]. 


References: 1: Marine Biology 96(3):375-383, 1987; 2: Polar Biology 9(7):461-465, 1989; 3: Biology of the Antarctic Seas XIII. Louis S. 
Kornicker, ed. Antarctic Research Series Volume 38. Washington, DC: American Geophysical Union, 1983. pp.1-60; 4: Comatulid 
Crinoids from R/V Eltanin Cruises in the Southern Oceans. Janis A. Speel. University Of Maine PhD dissertation. 1976; 5: Polar Biology 
16(5):309-320, 1996; 6: Tethys 6(3):631-653, 1974; 7: Revista Ciencia y Tecnologia del Mar 29(1):91-102, 2006; 8: Molecular Ecology 
21(10):2502-2518, 2012; 9: Diversity 15: 875, 2023 doi.org/10.3390/d15070875 


139